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Cellular and Molecular Life Sciences : CMLS|June 23, 2007
Extracellular microfibrils in development and diseaseF Ramirez, L Y Sakai, D B Rifkin, et al.Proceedings of the National Academy of Sciences of the United States of America|March 31, 1999
Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1L Pereira, S Y Lee, B Gayraud, et al.The Journal of Cell Biology|August 10, 2000
New insights into the assembly of extracellular microfibrils from the analysis of the fibrillin 1 mutation in the tight skin mouseB Gayraud, D R Keene, L Y Sakai, et al.Genomics|August 1, 1993
Fibrillin binds calcium and is coded by cDNAs that reveal a multidomain structure and alternatively spliced exons at the 5' endG M Corson, S C Chalberg, H C Dietz, et al.Nature Genetics|November 5, 1997
Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndromeL Pereira, K Andrikopoulos, J Tian, et al.Circulation Research|January 5, 2001
Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndromeT E Bunton, N J Biery, L Myers, et al.Genomics|August 1, 1993
Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndromeH C Dietz, I McIntosh, L Y Sakai, et al.The New England Journal of Medicine|July 21, 1994
A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndromeL Pereira, O Levran, F Ramirez, et al.American Journal of Human Genetics|July 1, 1995
Fifteen novel FBN1 mutations causing Marfan syndrome detected by heteroduplex analysis of genomic ampliconsG Nijbroek, S Sood, I McIntosh, et al.The Journal of Clinical Investigation|May 11, 1992
Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin geneH C Dietz, R E Pyeritz, E G Puffenberger, et al.Pageof 56